Atlas FDA

TEGTMEIER MAMMOMETER

FDA 510(k) clearance K792608 · decided 1980-01-04

Clearance details

K-number
K792608
Device name
TEGTMEIER MAMMOMETER
Applicant
Aztec Medical Products, Inc.
Decision
Substantially Equivalent
Date received
1979-12-18
Decision date
1980-01-04
Days to decision
17 days
Clearance type
Traditional
Advisory committee
Unknown
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.